Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5. (Q48390436)

11 February 2018

title

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5. (English)

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11 February 2018

lissencephaly with cerebellar hypoplasia

main subject

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lissencephaly

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cerebellar hypoplasia

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5

Ayelet Eran

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11 February 2018

Shay Tzur

9

object named as

Shay Tzur

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11 February 2018

author name string

Daniella Magen

1

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11 February 2018

Ayala Ofir

2

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11 February 2018

Liron Berger

3

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11 February 2018

Dorit Goldsher

4

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11 February 2018

Nasser Katib

6

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11 February 2018

Yousif Nijem

7

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11 February 2018

Euvgeni Vlodavsky

8

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11 February 2018

Doron M Behar

10

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11 February 2018

Yakov Fellig

11

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11 February 2018

Hanna Mandel

12

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11 February 2018

publication date

6 January 2015

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11 February 2018

published in

Human Genetics

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11 February 2018

volume

134

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11 February 2018

issue

3

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11 February 2018

page(s)

305-314

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11 February 2018

Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]

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Identifiers

DOI

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11 February 2018

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11 February 2018